Porous mullite ceramics with low thermal conductivity prepared by foaming and starch consolidation

Porous mullite ceramics were prepared from an industrial grade mullite powder by foaming and starch consolidation. The viscosities of the original suspensions and the foamed ones with solid loading of 62.5 and 67.5 wt% were measured. After the steps of forming and drying, the green bodies were sintered under different temperatures from 1,200 to 1,600 °C for 2 h. The influence of solid loading of suspension and sintering temperature on the porosity and compressive strength was evaluated. The sintered mullite ceramics, with porosity from 86 to 73 vol% and corresponding compressive strength from 1 to 22 MPa, contained a multi-modal microstructure with large spherical pores and small pores on internal walls. Thermal conductivity measurement carried out by the transient plane source technique at room temperature resulted in values as low as 0.09 W/mK. In addition, the relationship between thermal conductivity and porosity was discussed in detail.     

Digital light processing additive manufacturing of in situ mullite-zirconia composites

Digital light processing (DLP) can produce small series ceramic parts with complex geometries and tiny structures without the high cost of molds usually associated with traditional ceramic processing. However, the availability of feedstock of different ceramics for the technique is still limited. Mullite-zirconia composites are refractory materials with diverse applications, nevertheless, their 3D printing has never been reported. In this work, alumina and zircon were used as raw materials for additive manufacturing by DLP followed by in situ mullite and zirconia formation. Thus, coarse zircon powder was milled to submicrometric size, alumina-zircon photosensitive slurries were prepared and characterized, parts were manufactured in a commercial DLP 3D printer, debound, and sintered at different temperatures. The printed parts sintered at 1600 °C completed the reaction sintering and reached a flexural strength of 84 ± 13 MPa. The process proved capable of producing detailed parts that would be unfeasible by other manufacturing methods.     

Digital light processing stereolithography of zirconia ceramics: Slurry elaboration and orientation-reliant mechanical properties

Digital Light Processing (DLP) is a promising technique for the preparation of ceramic parts with complex shapes and high accuracy. In this study, 3 mol% yttria-stabilized tetragonal zirconia polycrystal (Y-TZP) UV-curable slurries were prepared and printed via DLP. Two different solid loadings (40.5 and 43.6 vol%, respectively) and printing directions were investigated to assess the influence of these parameters on physical and mechanical properties of the sintered parts. Zirconia samples were sintered at 1550 °C for 1 h, achieving a very high relative density (99.2%TD), regardless of solid loading and printing direction. FE-SEM micrographs shown a homogeneous and defect-free cross section with an average grains size of 0.56 ± 0.19 µm. Finally, mechanical properties were influenced by printing direction and zirconia vol%. Indeed, the composition with the higher solid loading (i.e. 43.6 vol%) had the highest three-point flexural strength (751 ± 83 MPa) when tested perpendicular to the printing plane.     

Synthesis and mechanical properties of mullite ceramics with coal gangue and wastes refractory as raw materials

With coal gangue and high alumina refractory solid wastes as raw materials, needle-like mullite powder, with an average diameter of about 1 μm, was synthesized at 1300°C by using the conventional solid-state reaction method. Mullite ceramics were derived from the inexpensive needle-like powder. Phase composition was examined by using X-ray diffraction (XRD), while morphologies of the ceramics were observed by using scanning electron microscopy. The content and distribution of elements in the sintered samples were characterized with energy dispersive spectrometer and X-ray fluorescence spectroscopy. Mechanical properties of the mullite ceramics were studied by using the three-point bending method. The aspect ratio of the needle-like mullite particles was up to 6. The mullite sample sintered at 1500°C for 3 hours had a density of 2.515 g·cm⁻³, which was slightly lower than the theoretical density. Maximum fracture toughness and bending strength of the mullite ceramics were 1.82 MPa·m^1/2 and 71.76 MPa, respectively. This study realizes the resource utilization of gangue and high alumina refractory solid wastes, and the prepared mullite ceramics have good application prospect.     

Effect of zirconia content on mechanical and thermal properties of mullite–zirconia composite

Abstract

Mullite–zirconia composites were prepared by adding various zirconia contents in the mullite ranging from 0 to 30 wt-% and sintering at 1400–1600°C for 2 h. The phase composition examined by X-ray diffraction showed that mullite was the major phase combined with developed t-ZrO₂ and m-ZrO₂ phase as a function of zirconia content, especially at 1600°C, wherein m-ZrO₂ predominated. Density increased when the zirconia content and sintering temperature were increased ranging from 2·2 to 3·53 g cm^?3. The morphology of mullite grain showed elongated grains, whereas dispersed zirconia showed equiaxed and intergranular grains. Flexural strength was continuously improved by adding zirconia during the sintering temperature ranging from 1400 to 1500°C, whereas flexural strength was initially improved up to 5 wt-% of zirconia addition and deteriorated with more than 5 wt-% of zirconia content during sintering between 1550 and 1600°C. The maximum strength, 190 MPa, was obtained when sintering mullite with 30 wt-% of zirconia content at 1500°C. The degradation of strength at high sintering temperature may be a result from more occurrence of m-ZrO₂ phase. Thermal expansion of sintered specimens indicated linear change and hysteresis loop change. The hysteresis loop obtained with increased zirconia content resulted in the t–m phase transformation. Martensitic start temperature M_s was determined to be 530°C for 15 wt-% zirconia sintered at 1500°C, implying that the t–m phase transformation occurred.     

Electrospun mullite nanofibers derived from diphasic mullite sol

Fine‐grained mullite nanofibers derived from the diphasic mullite sol were successfully fabricated by electrospinning and subsequent pyrolysis at 1500°C. Polymethylsiloxane and aluminum tri‐sec‐butoxide were selected as the silicon and aluminum source to synthesize the diphasic sol. Results show that the weight loss of mullite precursor fibers in our work was about 60 wt.%, which is similar with that of fibers fabricated using the monophasic sol. This low weight loss was mainly attributed to the high ceramic yield of polymethylsiloxane and low introduced polyvinylpyrrolidone content, which ensures the integrity of fiber morphology during the sintering process. Mullite fibers with 216 nm average diameter were fabricated after sintered at 1500°C and the corresponding grain size was only ~100 nm, much smaller than that in mullite fibers derived from monophasic sols. Therefore, it can be predicated that mullite fibers in this work should possess a higher mechanical strength than those derived from monophasic sols when the sintering temperature was higher than 1400°C and therefore was an ideal starting materials for the fabrication of mullite nanofibrous ceramics used as the high‐temperature thermal insulation materials.     

High-toughness mullite ceramics fabricated by hot-press sintering of pyrophyllite and AlOOH at low temperatures

High-toughness mullite ceramics were fabricated through hot-press sintering (HPS) of pyrophyllite and AlOOH, which were wet-milled and well mixed using a planetary ball mill. The impacts of sintering temperatures and contents of AlOOH on mullite phase formation, densification, microstructure and mechanical properties in ceramic materials were investigated through XRD, SEM and mechanical properties determination. The results indicated that high-toughness mullite ceramics could be successfully prepared by HPS at temperatures higher than 1200°C for 120 min. Increasing the sintering temperature from 1000 to 1300°C significantly enhanced the flexural strength and fracture toughness of samples. The highest flexural strength of 297.97±25.32 MPa and fracture toughness of 4.64±0.11 MPa⋅m^1/2 were obtained for samples sintered at 1300°C. Further increase of temperature to 1400°C resulted in slight decrease of flexural strength and fracture toughness. Compared with the mullite ceramics prepared only using pyrophyllite as raw material, incorporation of AlOOH into raw material significantly increased the mechanical properties of final mullite ceramics. And stoichiometric AlOOH and pyrophyllite as starting material gave the best performance in fracture toughness. The high-toughness of mullite ceramics were ascribed to the high mullite phase content, fine mullite whiskers and in situ formed, intertwined three-dimensional network structure obtained through HPS at a low temperature of 1300°C.     

Two alternative routes for starch consolidation of mullite green bodies

The starch consolidation forming method can be used in the manufacture of porous ceramics. In this method, based on swelling and gelatinization properties of starch in aqueous suspension at temperature (55–80 °C), the starch granules perform as both consolidator/binder of the green body and pore former at high-temperature.Commercially available powders of mullite and cassava starch were employed as raw materials. Mullite/starch aqueous suspensions (0.25 starch volume fraction of 40 vol.% total solid loading) were prepared by intensive mechanical mixing and homogenization in a ball mill.Two alternative forming routes of thermogelling mullite/starch aqueous suspensions—the Conventional Route (CR) and the Pre-Gelling Route (PGR)—were studied. With the CR, disks were formed by pouring the mullite/starch suspension at room temperature directly into metallic molds and heating at different temperatures (70 and 80 °C) and times (1 and 2 h). With the PGR, disks were shaped by pouring pre-gelled mullite/starch suspensions at 59 °C into heated molds and heating at the same experimental conditions. Once the consolidation process was finished, samples were removed of the mold and dried. Green bodies shaped by the two processing routes and obtained before (CR_bb and PGR_bb) and after (CR_ab and PGR_ab) burning out the starch, were characterized by bulk density and apparent porosity measurements and microstructural analysis by SEM/EDAX on the external and fracture surfaces. The homogeneity of the distribution of raw materials and pores, and the volume porosity were taken into account to establish the optimum consolidation conditions to be used in the preparation of mullite porous materials with homogeneous microstructures.     

Impact of microwave processing on porcelain microstructure

Microstructural evolution on sintering of porcelain powder compacts using microwave radiation was compared with that in conventionally sintered samples. Using microwaves sintering temperature was reduced by ~ 75 °C and dwell time from 15 min to 5 min while retaining comparable physical properties i.e. apparent bulk density, water absorption to conventionally sintered porcelain. Porcelain powder absorbed microwave energy above 600 °C due to a rapid increase in its loss tangent. Mullite and glass were used as indicators of the microwave effect: mullite produced using microwaves had a nanofibre morphology with high aspect ratio (~ 32 ± 3:1) believed associated with a vapour-liquid-solid (VLS) formation mechanism not previously reported. Microwaves also produced mullite with different chemistry having ~ 63 mol% alumina content compared to ~ 60 mol% alumina in conventional sintered porcelain. This was likely due to accelerated Al⁺³ diffusion in mullite under microwave radiation. Liquid glass was observed to form at relatively low temperature (~ 900–1000 °C) using microwaves when compared to conventional sintering which promoted the porcelains ability to absorb them.     

Comparative study of conventional and microwave sintered mullite fibres: structural study

Mullite fibres were synthesised from a mixture of aluminium, aluminium chloride and acidic silica solutions as monophasic salts using a sol–gel technique. The viscosity and rheological behaviour of the mullite precursor sol were examined. Mullite fibres were synthesised using both conventional and microwave sintering techniques. The samples were characterised by X-ray diffraction and scanning electron microscopy. Pure mullite fibres were synthesised by microwave sintering at a relatively low temperature of 1200°C. The grain size of the fibre samples sintered using the microwave technique was finer than that produced by conventional sintering. These results show that microwave sintering is a promising technique for processing mullite fibres.     

Microstructure and Mechanical Properties of Mullite Prepared by the Sol-Gel Method

Mullite (3Al₂O₃·2SiO₂) of stoichiometric composition was prepared by mixing boehmite sol and silica dispersion and gelling at a pH of 3. Complete mullitization takes place at or above 1300°C. Ultrafine mullite powder prepared by calcining gel at 1400°C and attrition milling could be sintered to >98% (theoretical density) at 1650°C for 1.5 h. The flexural strength of the sintered body at room temperature was 405 MPa and 350 MPa at 1300°C. Only traces of a secondary phase were observed along the grain boundary.     

Thermal conductivities and mechanical properties of AlN ceramics fabricated by three dimensional printing

AlN ceramics were successfully fabricated through a joint process of digital light processing (DLP) 3D printing technology and heat treatment at 1780 °C∼1845 °C. DLP is an addictive manufacturing process, enabling the near net shape fabrication. The AlN grains in this work developed well and there were small amounts of grain-boundary phases at the three-grain junctions. The particle size of AlN became larger and the densification increased with increasing sintering temperature. The pores of AlN ceramics also decreased, which led to the increase of thermal conductivity and flexural strength. The optimal thermal conductivity and flexural strength of AlN ceramic reached 155 W/(m·K) and 265 ± 20 MPa when sintered at 1845 °C.     

Mullite/ β-spodumene composites: Preparation and characterization

Mullite/ β-spodumene composites were fabricated by the addition of 5 up to 20 mass% β -spodumene powder to mullite matrix. Both mullite and β-spodumene were prepared by sol-gel technique. The batches were uniaxially pressed into discs and rectangular bars, then pressureless sintered at 1400 °C up to 1700 °C for 1 h. Mechanical and thermal properties, as well as microstructure and phase composition were carried out on the sintered composites. The results show that although the increase in the soft β-spodumene reduces the hardness and the thermal expansion of the composites, they lower the firing temperature and enhance the flexural strength. The study indicates that β-spodumene content has a noticeable effect on the composites thermal expansion coefficient. It also shows that it is possible to tailor mullite/ β-spodumene composite with adjusted thermal expansion coefficient by changing the mullite to β-spodumene ratio.     

Sintering and microstructural study of mullite prepared from kaolinite and reactive alumina: Effect of MgO and TiO2

Mullite ceramic was prepared using kaolinite and synthesized alumina (combustion route) by solid-state interaction process. The influence of TiO₂ and MgO additives in phase formation, microstructural evolution, densification, and mechanical strengthening was evaluated in this work. TiO₂ and MgO were used as sintering additives. According to the stoichiometric composition of mullite (3Al₂O₃·2SiO₂), the raw materials, ie kaolinite, synthesized alumina, and different wt% of additives were wet mixed, dried, and uniaxially pressed followed by sintering at different temperature. 1600°C sintered samples from each batch exhibit enhanced properties. The 1 wt% TiO₂ addition shows bulk density up to 2.96 g/cm³ with a maximum strength of 156.3 MPa. The addition of MgO up to 1 wt% favored the growth of mullite by obtaining a density and strength matching with the batch containing 1 wt% TiO₂. These additives have shown a positive effect on mullite phase formation by reducing the temperature for complete mullitization by 100°C. Both additives promote sintering by liquid phase formation. However, the grain growth, compact microstructure, and larger elongated mullite crystals in MgO containing batch enhance its hardness properties.     

Mullite fibres prepared by sol–gel method using polyvinyl butyral

Mullite fibres with uniform diameter and smooth surface have been synthesized using commercial grade polyvinyl butyral (PVB) as binder. The sol with good spinnablity was obtained at reaction temperature of 60 °C for 1 h. The results of X-ray diffraction indicated that the Al–Si spinel was obtained before complete mullization, which implied the addition of PVB retarded the phase transformation of mullite. The fibres showed a rough surface and lateral cracks at 800 °C. Smooth and dense surface was observed when fibres were sintered at 1200 °C and completed transformation to mullite was achieved. This technique offered the possibility of synthesizing mullite fibres at considerably lower cost than at present.     

Mechanical and thermal behavior of cellular mullite materials

In this paper, the mechanical behavior and thermal properties of cellular mullite bodies obtained by thermal direct-consolidation of foamed aqueous suspensions of mullite-bovine serum albumin (BSA) and mullite-BSA-methylcellulose (MC) were studied. The mechanical behavior of cellular mullite materials sintered at 1600 °C was evaluated by diametral compression at room temperature, 1000 °C and 1300 °C. The variation in the thermal diffusivity and thermal conductivity at temperatures up to 900 °C was determined using the laser-flash method. The results of the mechanical and thermal evaluation were analyzed based on the porosity features of the sintered materials, which was determined in turn by the starting system used for shaping the bodies.     

Phase Evolution,Microstructure, and Mechanical Properties of Alumina–Mullite–Zirconia Composites Prepared by Iranian Andalusite

This paper investigates the effects of Iranian andalusite and short milling times on alumina–mullite–zirconia composites. Andalusite powder was added at 0, 2.5, 5, and 10 wt% to an alumina–zircon mixture and the raw materials were milled for 1 or 3 h. The sintering of samples was carried out at the temperatures of 1550°C, 1600°C, and 1650°C for 3 h. Microstructural changes, phase composition, physical properties, and mechanical strength of the sintered composites were characterized by scanning electron microscopy, X‐ray diffraction, density, and strength measurement tests. Results show that andalusite promoted the decomposition of zircon and accelerated the reaction sintering of alumina–zircon, which leads to the formation of much more mullite phase and improvements to the composites’ thermal shock resistance up to about 50%.     

Reliable high strength alumina fabricated by DCC-HVCI using submicron calcium citrate complex

Ceramics with high strength and reliability are highly demanded in engineering applications. In this paper, a modified direct coagulation casting via high valence counter ions (DCC-HVCI) method for alumina using calcium citrate complex assisted by glycerol diacetate was investigated. Calcium citrate complex suspensions were prepared by mixing tri-ammonium citrate and calcium chloride in water. Effect of reaction time on the chelating properties of the prepared suspensions was investigated. Concentrated alumina suspensions with a solid loading of 50 vol% were prepared by mixing the calcium citrate complex suspensions and alumina powder at pH of 10.5. Then the suspensions were coagulated by adding 3–6 vol% glycerol diacetate at temperatures of 40–70 °C for 2–6 h. The compressive strength of the coagulated wet samples is in the range 1.1–2.4 MPa. Alumina ceramics sintered at 1550 °C shows homogeneous microstructures with flexural strength and Weibull modulus of 455±17 MPa and 30, respectively.     

Development and evaluation of Al2O3–ZrO2 composite processed by digital light 3D printing

Digital Light Processing (DLP) is a promising approach to fabricate delicate ceramic components with high-fidelity structural features. In this work, the alumina and zirconia/alumina ceramic suspensions with low viscosity and high solid loading (40 vol%) were prepared specifically for DLP 3D printing. After debinding and sintering, the final parts were obtained without any defects. The surface morphologies and mechanical properties of alumina (Al₂O₃) and zirconia toughened alumina (ZTA) composites were investigated and the results showed that the final parts exhibited high relative densities and good interlayer combination at the sintering temperature of 1600 °C. Comparing with the Al₂O₃, the ZTA composites exhibited significantly enhanced density (99.4%), bending strength (516.7 MPa) and indentation fracture toughness (7.76 MPa m^1/2).     

Preparation of Mullite Cordierite Composite Powders by the Sol-Gel Method: Its Characteristics and Sintering

Mullite/cordierite composite powders containing different proportions of cordierite were prepared by the sol-gel method using boehmite, colloidal silica, and Mg(NO₃)₂·6H₂O. Mullite and cordierite sols were prepared separately and mixed to form the composite sol. Mullitization temperature depends on the cordierite content in the composite. Also, α-cordierite crystallizes at a lower temperature in a mullite-rich (MC20) composite. The XRD patterns of the powders calcined at 1450°C for 12 h showed that mullite and cordierite exist as two different phases, and no additional phases were observed. The IR absorbance spectra of composites showed characteristic peak corresponding to both mullite and cordierite. The sintered density of the powders increases with temperature up to 1450°C and decreases beyound the melting point of cordierite (1455°C). The microstructure of MC30 sintered at 1440°C for 3 h consisted of acicular grains, whereas in MC40 and MC50 equiaxed grain morphology was observed under similar sintering conditions. The flexural strength and Vickers hardness decreases with the increase of cordierite content in the composite. Dielectric constant and thermal expansion showed a similar behavior.